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Person
Person

Person

Anna Köttgen (1974-)

Name

Anna Köttgen

Time

1974- (Date of birth and death)

Place

Freiburg im Breisgau (Wirkungsort)
Baltimore, Md. (Wirkungsort)
Deutschland
USA

Gender

weiblich

Academic degree

Prof. Dr. (Universität Freiburg, Medizinische Fakultät) (2002)

Variant

A. Köttgen
Anna Kottgen
Anna Hopf (früherer Name)

Related

Albert-Ludwigs-Universität Freiburg. Medizinische Fakultät (2010-)
Johns Hopkins Bloomberg School of Public Health (2005-2015)

Further information

Laufbahn am Universitätsklinikum Freiburg: Emmy Noether-Gruppenleiterin (2010-2015), Heisenberg-Professorin (W3, seit 2016) und Leiterin des Instituts für Genetische Epidemiologie (seit 2017)

Source

ResearchGate: https://www.researchgate.net/profile/Anna-Koettgen (Stand: 07.08.2024)
https://www.med.uni-freiburg.de/de/fakultaet/profs/akoettgen (Stand: 07.08.2024)

Record type

Person

GND-Identifier

123510333

Record ID

123510333

Involved in

show all

SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans

The pathogenesis of gout: molecular insights from genetic, epigenomic and transcriptomic studies

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

Apolipoprotein A-IV concentrations and cancer in a large cohort of chronic kidney disease patients: results from the GCKD study

Associations of baseline and longitudinal serum uromodulin with kidney failure and mortality: results from the African American Study of Kidney Disease and Hypertension (AASK) trial

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury

Epigenome-wide DNA methylation in unipolar depression - predictive biomarker of antidepressant treatment response?

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Integrating multiple kidney function markers to predict all-cause and cardiovascular disease mortality: prospective analysis of 366 758 UK Biobank participants

Lipoprotein(a) concentrations and cardiovascular disease in patients with chronic kidney disease: results from the German Chronic Kidney Disease study

Long term outcomes of patients with IgA nephropathy in the German CKD (GCKD) cohort

Long-term outcomes of adults with FSGS in the German Chronic Kidney Disease cohort

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

New insights into the hypothalamic–pituitary–thyroid axis: a transcriptome- and proteome-wide association study

SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans

X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

A polygenic score for reduced kidney function and adverse outcomes in a cohort with chronic kidney disease

Association of mineral and bone biomarkers with adverse cardiovascular outcomes and mortality in the German Chronic Kidney Disease (GCKD) cohort

Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohorts

Clonal hematopoiesis of indeterminate potential and kidney function decline in the general population

Copeptin, natriuretic peptides, and cardiovascular outcomes in patients with CKD: the German Chronic Kidney Disease (GCKD) study

Differential prognostic utility of adiposity measures in chronic kidney disease

Differential Prognostic Utility of Adiposity Measures in Chronic Kidney Disease

Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank

KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study

Mapping of the gene network that regulates glycan clock of ageing

Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations

Prospective cohort study of soluble urokinase plasminogen activation receptor and cardiovascular events in patients with CKD

Prospective Cohort Study of Soluble Urokinase Plasminogen Activation Receptor and Cardiovascular Events in Patients With CKD

Regional variation in hemoglobin distribution among individuals with CKD: the ISN international network of CKD cohorts

Regional Variation in Hemoglobin Distribution Among Individuals With CKD: the ISN International Network of CKD Cohorts

SLC26A1 is a major determinant of sulfate homeostasis in humans

Wildtype heterogeneity contributes to clonal variability in genome edited cells

A slit-diaphragm-associated protein network for dynamic control of renal filtration

A saturated map of common genetic variants associated with human height

A slit-diaphragm-associated protein network for dynamic control of renal filtration

An intermediate-effect size variant in UMOD confers risk for chronic kidney disease

Apolipoprotein A‐IV concentrations and clinical outcomes in a large chronic kidney disease cohort: results from the GCKD study

Bucket fuser: statistical signal extraction for 1D 1H NMR metabolomic data

Cardiovascular disease protein biomarkers are associated with kidney function: The Framingham Heart Study

Clock genes rescue nphp mutations in zebrafish

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

Epigenome-wide DNA methylation in obsessive-compulsive disorder

Framework and baseline examination of the German National Cohort (NAKO)

Framework and baseline examination of the German National Cohort (NAKO)

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Genetics of osteopontin in patients with chronic kidney disease: the German chronic kidney disease study

Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases

High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases

Mild-to-moderate kidney dysfunction and cardiovascular disease: observational and mendelian randomization analyses

The effect of LPA Thr3888Pro on lipoprotein(a) and coronary artery disease is modified by the LPA KIV-2 variant 4925G>A

Wildtype heterogeneity contributes to clonal variability in genome edited cells
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